A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17860197



Internal ID22043840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20945303..20945303hg38UCSC Ensembl
chr7:20984922..20984922hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6261155
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17860197
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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